Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs17782313 0.683 0.480 18 60183864 intergenic variant T/C snv 0.24 34
rs12826786 0.683 0.480 12 53961717 upstream gene variant C/T snv 0.38 26
rs10811661 0.724 0.400 9 22134095 intergenic variant T/C snv 0.14 22
rs2046210 0.708 0.280 6 151627231 intergenic variant G/A snv 0.41 21
rs7931342 0.689 0.360 11 69227030 intergenic variant T/G snv 0.58 20
rs642961 0.732 0.440 1 209815925 intergenic variant A/G snv 0.84 14
rs874945 0.732 0.240 12 53961667 upstream gene variant C/T snv 0.38 14
rs889312 0.732 0.360 5 56736057 regulatory region variant C/A snv 0.69 14
rs10811474 0.742 0.240 9 21114238 intergenic variant A/G snv 0.44 11
rs10941679 0.763 0.120 5 44706396 intergenic variant A/G snv 0.25 11
rs13293512 0.763 0.360 9 94167461 intron variant T/C snv 0.24 11
rs1111875 0.776 0.360 10 92703125 intergenic variant C/T snv 0.36 10
rs2069514 0.807 0.160 15 74745879 upstream gene variant G/A snv 0.13 9
rs7907606 0.790 0.120 10 103920874 upstream gene variant T/G snv 0.26 8
rs10090154 0.807 0.160 8 127519892 intergenic variant T/A;C snv 7
rs10896449 0.827 0.200 11 69227200 intergenic variant A/G snv 0.53 7
rs132793 0.851 0.160 22 41667677 downstream gene variant A/C;G;T snv 7
rs4849887 0.807 0.080 2 120487546 intergenic variant T/A;C snv 7
rs6013897 0.790 0.200 20 54125940 regulatory region variant T/A snv 0.23 7
rs2410373 0.851 0.120 8 16066997 intergenic variant A/C snv 0.34 6
rs2736108 0.807 0.160 5 1297373 upstream gene variant C/T snv 0.24 6
rs4415084 0.827 0.080 5 44662413 upstream gene variant C/T snv 0.49 6
rs7166081 0.925 0.080 15 67199963 downstream gene variant G/A snv 0.76 6
rs9325782 0.851 0.120 8 16232964 intron variant C/T snv 0.87 6